Difference between revisions of "Ontology Development Progress Report December 2014"
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===Improved Biological Representation===
===Improved Biological Representation===
Revision as of 12:20, 10 December 2014
Ontology Development Progress Report
GOC Meeting Dec 2014
Prepared and Submitted by Jane Lomax and David Hill
- David Hill (MGI)
- Tanya Berardini (TAIR)
- Heiko Dietze (LBL)
- Harold Drabkin (MGI)
- Becky Foulger (EBI) (left Jan 2014)
- Jane Lomax (EBI)
- Chris Mungall (LBL)
- David Osumi-Sutherland (EBI)
- Paola Roncaglia (EBI)
SF items opened (SF items closed)
|Jan 2014||39 (44)|
|Feb 2014||50 (81)|
|Mar 2014||59 (41)|
|Apr 2014||74 (52)|
|May 2014||71 (75)|
|Jun 2014||79 (70)|
|Jul 2014||66 (58)|
|Aug 2014||76 (115)|
|Sept 2014||110 (52)|
|Oct 2014||52 (73)|
|Nov 2014||83 (69)|
|Dec 2014||26 (5)|
|Total 2014||746 (691)|
Total number of GO terms added Jan 2014 to Dec 2,2014: 1868
Total number of GO terms added manually Jan 2014 to Dec. 2,2014: 549 Total number of GO terms added via TermGenie template Jan 2014 to Dec 2,2014: 1046 Total number of GO terms added via TermGenie freeform Jan 2014 to Dec 2,2014: 273
Total number of GO terms obsoleted Jan 2014 to Dec 2,2014: obsolete 57, merged 34
Transition to OWL
Ontology editors are routinely using the OWL version of GO to check for logical consistency in the ontology and to create terms with logical definitions. OWL is also used as the underlying format for creating new terms via the termgenie tool.
Since Jan 2014 we have added 6 new templates to our template-based term addition tool, TermGenie. These are:
- cell_migration (CL)
- biosynthesis_from (CHEBI)
- biosynthesis_via (CHEBI)
- catabolism_to (CHEBI)
- catabolism_via (CHEBI)
- metazoan_development (UBER)
templates with additional functionality:
- add plant cells for cell_differentiation (PO)
- add option to also create transmembrane transport for chemical
transport from to (CHEBI)
These templates utilize both classes within GO and classes from external ontologies, shown in parentheses. PO = plant ontology, CL = cell ontology, CHEBI = chemicals of biological interest ontology, UBER= Uberon.
The ontology group has been working in coordination with the annotation group to refine and clarify the use of relations in annotation extensions. This ongoing work requires identifying a set of well-defined easy-to-use relations that will integrate with the relation ontology (RO) and will be used consistently in the ontology and by gene annotators. These relations will be used in accordance with future annotation models using the common annotation tool and will permit the folding and unfolding of contextual data.
Improved Biological Representation
We developed design patterns for transport processes with specification of start and end location and barriers transported across as well as the nature of the entity transported. Newly added OWL axioms allow inference of start and end location over part relations in the GO. 11 different TermGenie templates for transport processes are now available to users.
We developed design patterns for classes used to record the relationship of proteins and protein complexes to membranes (integral, anchored, peripheral etc).
Ontology work was carried out to clean up and revise the ‘execution of apoptosis’ node. This was accompanied by a re-annotation effort and by addition of documentation to the apoptosis curation manual (http://wiki.geneontology.org/index.php/Apoptosis_Curation_Manual). Further discussion was carried out about the general ‘cell death’ term.
This ontology development project is run in collaboration with the SYSCILIA Consortium (http://syscilia.org). It aims at reviewing and enriching the GO to better represent ciliary substructures in the cell (CC branch) as well as processes that cilia are involved in (BP branch). This is especially relevant as research on ciliary functions and ciliopathies is an emerging area of biomedical study. 51 terms were added or revised, mostly in the CC branch; work on the BP branch will take place in 2015 depending on resources.
This work aims at extending the GO CC branch to cover unicellular species that have specialized, yet-unrepresented subcellular structures. The Giardia project is run in collaboration with Scott Dawson's lab at UC Davis. 33 new terms have been added so far to aid annotation of protein localization to structures unique to Giardia species (unicellular protozoan parasites). Giardiasis is the most common pathogenic parasitic infection in humans worldwide. Another taxonomic group with distinct cellular substructures is that of Dinophyceae (Dinoflagellates), flagellate protists with >2,000 living species. 10 new GO terms have been added to represent dinoflagellate-specific structures, in collaboration with Anne Thessen, with a few more requested recently.
This project aims at revising and enriching the GO to include new extracellular RNA-related terms. This work is carried out in collaboration with the Extracellular RNA Communication Consortium (ERCC), with feedback from the International Society for Extracellular Vesicles (ISEV) and American Society for Exosomes and Microvesicles (ASEMV), as well as input from the wider extracellular vesicle (EV) community. Discussion is underway and we anticipate that the new terms will be added early in 2015.
The ontology work on this project has reached completion. There are now total of 344 classes under ‘viral process’ (GO:0016032) and 65 classes of ‘virion part’ (GO:0044423). A viral GO slim was also created. A paper 'Representing microbe-host interactions in the Gene Ontology' Foulger & Lomax et. al. has been submitted to BMC Microbiology.
Metabolic Pathways (Glycolysis)
The representation of glycolytic pathways is now complete in the ontology and we have begun working on the representation of glycolytic fermentation using the existing glycolysis framework.